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rs761064915

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs761064915(A;A)
Make rs761064915(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position3498966
GeneASPA, SPATA22
is asnp
is mentioned by
dbSNPrs761064915
ebirs761064915
HLIrs761064915
Exacrs761064915
Varsomers761064915
Maprs761064915
PheGenIrs761064915
hapmaprs761064915
1000 genomesrs761064915
hgdprs761064915
ensemblrs761064915
gopubmedrs761064915
geneviewrs761064915
scholarrs761064915
googlers761064915
pharmgkbrs761064915
gwascentralrs761064915
openSNPrs761064915
23andMers761064915
23andMe allrs761064915
SNP Nexus

SNPshotrs761064915
SNPdbers761064915
MSV3drs761064915
GWAS Ctlgrs761064915
Max Magnitude0
ClinVar
Risk rs761064915(A;A)
Alt rs761064915(A;A)
Reference rs761064915(G;G)
Significance Probable-Pathogenic
Disease Spongy degeneration of central nervous system
Variation info
Gene SPATA22 ASPA
CLNDBN Spongy degeneration of central nervous system
Reversed 0
HGVS NC_000017.10:g.3402260G>A
CLNSRC
CLNACC RCV000169117.1,